Immunoaffinity Chromatography

Timothy A. Springer1

1 Center for Blood Research Harvard Medical School, Boston
Publication Name:  Current Protocols in Protein Science
Unit Number:  Unit 9.5
DOI:  10.1002/0471140864.ps0905s03
Online Posting Date:  May, 2001
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Abstract

This unit describes the isolation of soluble or membrane‐bound protein antigens from cells or homogenized tissue by immunoaffinity chromatography. This technique involves the elution of a single protein from an immunoaffinity column after prior elution of nonspecifically adsorbed proteins. Specifically, antibodies are coupled to Sepharose (an insoluble, large‐pore‐size chromatographic matrix). High‐molecular‐weight antigens pass freely into and out of the pores and bind to antibodies covalently bound to the matrix. To elute the bound antigen from the immunoaffinity matrix, the antibody‐antigen interaction is destabilized by brief exposure to high‐ or low‐pH buffer. Batch purification of antigens is provided as an alternate procedure that shortens the column loading time. The detergent octyl β‐D‐glucoside can be used instead of Triton X‐100 for elution. Because octyl β‐D‐glucoside has a high critical micelle concentration (CMC), a protocol is provided for its removal by dialysis. The procedure for covalently linking an antibody to Sepharose using the cyanogen bromide activation method is given in a support protocol.

     
 
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Table of Contents

  • Basic Protocol 1: Isolation of Soluble or Membrane‐Bound Antigens
  • Alternate Protocol 1: Low‐pH Elution of Antigens
  • Alternate Protocol 2: Batch Purification of Antigens
  • Alternate Protocol 3: Elution in Octyl β‐D‐Glucoside
  • Support Protocol 1: Preparation of Antibody‐Sepharose
  • Reagents and Solutions
  • Commentary
  • Figures
     
 
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Materials

Basic Protocol 1: Isolation of Soluble or Membrane‐Bound Antigens

  Materials
  • Antibody (Ab)‐Sepharose (see protocol 5)
  • Activated, quenched (control) Sepharose, prepared as for Ab‐Sepharose (see protocol 5) but eliminating Ab or substituting irrelevant Ab during coupling
  • Cells or homogenized tissue
  • Tris/saline/azide (TSA) solution (see recipe), ice cold
  • Lysis buffer (see recipe), ice cold
  • 5% (w/v) sodium deoxycholate (Na‐DOC; filter sterilize and store at room temperature)
  • Wash buffer (see recipe)
  • Tris/Triton/NaCl buffers, pH 8.0 and 9.0 (see recipe), ice‐cold
  • Triethanolamine solution (see recipe), ice cold
  • 1 M Tris·Cl, pH 6.7 ( appendix 2E), ice cold
  • Column storage solution (see recipe), ice cold
  • Chromatography columns
  • Ultracentrifuge
  • Quick‐seal centrifuge tubes (Beckman)
  • Additional reagents and equipment for column chromatography (units 8.1), SDS‐PAGE (unit 10.1), and silver staining (unit 10.5)
NOTE: Carry out all procedures involving antigen in a 4°C cold room or on ice.

Alternate Protocol 1: Low‐pH Elution of Antigens

  • Sodium phosphate buffer, pH 6.3 (see recipe)
  • Glycine buffer (see recipe)
  • 1 M Tris·Cl, pH 9.0 ( appendix 2E)

Alternate Protocol 2: Batch Purification of Antigens

  • TSA solution (see recipe) containing 1% octyl β‐D‐glucoside

Alternate Protocol 3: Elution in Octyl β‐D‐Glucoside

  Materials
  • 1 to 30 mg/ml antigen‐specific monoclonal or polyclonal antibody
  • 0.1 M NaHCO 3/0.5 M NaCl
  • Sepharose CL‐4B (or Sepharose CL‐2B for high‐molecular‐weight antigens; Pharmacia Biotech)
  • 2 M Na 2CO 3
  • Cyanogen bromide (CNBr)/acetonitrile (see recipe)
  • 1 mM and 0.1 mM HCl, ice‐cold
  • 0.05 M glycine (or ethanolamine), pH 8.0
  • Tris/saline/azide (TSA) solution (see recipe)
  • Dialysis tubing (MWCO >10,000)
  • Ultracentrifuge
  • Whatman no. 1 filter paper
  • Buchner funnel
  • Erlenmeyer filtration flask
  • Water aspirator
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Figures

Videos

Literature Cited

Literature Cited
   Cuatrecasas, P. 1970. Protein purification by affinity chromatography. J. Biol. Chem. 245:3059‐3065.
   Ey, P.L., Prowse, S.J., and Jenkin, C.R. 1978. Isolation of pure IgG1, IgG2a and IgG2b immunoglobulins from mouse serum using protein A–Sepharose. Immunochemistry 15:429‐436.
   Gelb, W.G. 1973. Affinity chromatography: For separation of biological materials. Am. Lab. 81:61‐67.
   Helenius, A., McCaslin, D.R., Fries, E., and Tanford, C. 1979. Properties of detergents. Methods Enzymol. 56:734‐749.
   Johnson, P., Williams, A.F., and Woollett, G.R. 1985. Purification of membrane glycoproteins with monoclonal antibody affinity columns. In Hybridoma Technology in the Biosciences and Medicine (T.A. Springer, ed.) pp. 163‐175. Plenum, New York.
   Kürzinger, K. and Springer, T.A. 1982. Purification and structural characterization of LFA‐1, a lymphocyte function‐associated antigen, and Mac‐1, a related macrophage differentiation antigen. J. Biol. Chem. 257:12412‐12418.
   March, S.C., Parikh, I., and Cuatrecasas, P. 1974. A simplified method for cyanogen bromide activation of agarose for affinity chromatography. Anal. Biochem. 60:149‐152.
   Plunkett, M.L. and Springer, T.A. 1986. Purification and characterization of the lymphocyte function‐associated‐2 (LFA‐2) molecule. J. Immunol. 136:4181‐4187.
   Rivnay, B., Wank, S.A., Poy, G., and Metzger, H. 1982. Phospholipids stabilize the interaction between the alpha and beta subunits of the solubilized receptor for immunoglobulin E. Biochemistry 21:6922‐6927.
   Schroeder, R., London, E., and Brown, D. 1994. Interactions between saturated acyl chains confer detergent resistance on lipids and glycosylphosphatidylinositol (GPI)‐anchored proteins: GPI‐anchored proteins in liposomes and cells show similar behavior. Proc. Natl. Acad. Sci. U.S.A. 91:12130‐12134.
   Tsuchiya, T. and Saito, S. 1984. Use of n‐octyl‐β‐D‐thioglucoside, a new nonionic detergent, for solubilization and reconstitution of membrane proteins. J. Biochem. 96:1593‐1597.
   Wilchek, M., Miron, T., and Kohn, J. 1984. Affinity chromatography. Methods Enzymol. 104:3‐55.
   Williams, A.F. and Barclay, A.N. 1986. Glycoprotein antigens of the lymphocyte surface and their purification by antibody affinity chromatography. In Immunological Methods in Biomedical Sciences (D.M. Weir, L.A. Herzenberg, C.C. Blackwell, and L.A. Herzenberg, eds.) pp. 22.1‐22.24. Blackwell Scientific, Oxford.
Key References
   Harlow, E. and Lane, D. 1988. Antibodies: A Laboratory Manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.
  Describes the critical parameters involved in immunoaffinity chromatography.
   Hjelmeland, J.M. and Chrambach, A. 1984. Solubilization of functional membrane proteins. Methods Enzymol. 104:305‐318.
  Describes the mechanism of activation of Sepharose by CNBr and alternative activation procedures, and lists numerous examples of proteins purified by affinity chromatography.
   Johnson et al., 1985. See above.
   Wilchek et al., 1984. See above.
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